Tenley Nathan, Corn David J, Yuan Lewis, Lee Zhenghong
Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA.
Department of Biomedical Engineering, Case Western Reserve University, Cleveland, OH 44106, USA ; Department of Radiology, University Hospitals Case Medical Center, Cleveland, OH 44106, USA.
J Cancer Ther. 2013 Apr;4(2):561-567. doi: 10.4236/jct.2013.42071.
The clinical utility of positron emission tomography (PET) imaging for liver cancer applications is not clearly defined either for diagnosis or treatment assessment. Previous clinical studies demonstrated that fluorodeoxyglucose (FDG) did not show uptake in some hepatocellular carcinoma (HCC) while acetate showed uptake. Pre-imaging fasting is required for clinical PET imaging with FDG. No studies were done to confirm the effect of fasting on acetate uptake in HCC for PET imaging. We investigated this situation with a woodchuck model of viral infection-induced HCC.
Four tumor-bearing and one control woodchucks were involved in this study. They were first imaged by PET in fed state followed by another imaging session one week later when they were fasted over-night. Some animals also had FDG-PET scan that was acquired later on the same day. After imaging studies, animals were sacrificed, and their liver excised for histology. Standardized Uptake Value (SUV) was calculated using a region of interest (ROI) placed on each tumor with focal uptake.
Acetate showed uptake in each HCC lesion when the animals were either fasted or fed with no significant difference in SUV values (=0.177); some of the tumors were histologically confirmed as well-differentiated HCC while others were confirmed as moderately- or poorly-differentiated HCC; no focal uptake was found in the control animal. For the accompanying FDG scans, the uptake was detected only in animals that were fasted although the uptake pattern was different from that with acetate.
This study provided a hint that fasting or not has little impact on PET imaging of HCC with acetate. It also confirmed prior finding regarding tumor heterogeneity that led to different tracer uptake pattern in the same tumor. Human studies are needed to validate the findings from this pre-clinical investigation.
正电子发射断层扫描(PET)成像在肝癌应用中的临床效用,无论是用于诊断还是治疗评估,都尚未明确界定。先前的临床研究表明,氟脱氧葡萄糖(FDG)在一些肝细胞癌(HCC)中未显示摄取,而乙酸盐显示有摄取。使用FDG进行临床PET成像需要在成像前禁食。尚未进行研究来证实禁食对HCC中乙酸盐摄取用于PET成像的影响。我们用病毒感染诱导的HCC土拨鼠模型研究了这种情况。
本研究涉及4只荷瘤土拨鼠和1只对照土拨鼠。它们首先在进食状态下进行PET成像,然后在一周后过夜禁食时进行另一次成像。一些动物还在同一天晚些时候进行了FDG-PET扫描。成像研究后,处死动物,切除肝脏进行组织学检查。使用放置在每个有局灶性摄取的肿瘤上的感兴趣区域(ROI)计算标准化摄取值(SUV)。
无论动物是禁食还是进食,乙酸盐在每个HCC病变中均显示摄取,SUV值无显著差异(P = 0.177);一些肿瘤经组织学证实为高分化HCC,而其他肿瘤经证实为中分化或低分化HCC;对照动物未发现局灶性摄取。对于伴随的FDG扫描,仅在禁食的动物中检测到摄取,尽管摄取模式与乙酸盐不同。
本研究提示禁食与否对HCC用乙酸盐进行PET成像影响不大。它还证实了先前关于肿瘤异质性的发现,即同一肿瘤中导致不同示踪剂摄取模式的原因。需要进行人体研究来验证这项临床前研究的结果。